WO2009115972A1 - Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes - Google Patents

Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes Download PDF

Info

Publication number
WO2009115972A1
WO2009115972A1 PCT/IB2009/051068 IB2009051068W WO2009115972A1 WO 2009115972 A1 WO2009115972 A1 WO 2009115972A1 IB 2009051068 W IB2009051068 W IB 2009051068W WO 2009115972 A1 WO2009115972 A1 WO 2009115972A1
Authority
WO
WIPO (PCT)
Prior art keywords
influenza
virus
monoclonal antibody
subtypes
chain variable
Prior art date
Application number
PCT/IB2009/051068
Other languages
English (en)
French (fr)
Inventor
Roberto Burioni
Massimo Clementi
Original Assignee
Pomona Biotechnologies Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40293277&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2009115972(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to ES09722394T priority Critical patent/ES2544968T5/es
Priority to NZ588238A priority patent/NZ588238A/xx
Priority to DK09722394.5T priority patent/DK2274335T3/en
Priority to JP2011500336A priority patent/JP5542118B2/ja
Priority to EA201071087A priority patent/EA027069B1/ru
Priority to CA2718923A priority patent/CA2718923C/en
Priority to CN200980117842.2A priority patent/CN102037013B/zh
Priority to MX2010010120A priority patent/MX2010010120A/es
Priority to BRPI0909123A priority patent/BRPI0909123B8/pt
Priority to PL09722394T priority patent/PL2274335T3/pl
Priority to US12/922,850 priority patent/US9200063B2/en
Priority to AU2009227567A priority patent/AU2009227567B2/en
Priority to EP09722394.5A priority patent/EP2274335B2/en
Application filed by Pomona Biotechnologies Llc filed Critical Pomona Biotechnologies Llc
Publication of WO2009115972A1 publication Critical patent/WO2009115972A1/en
Priority to ZA2010/06934A priority patent/ZA201006934B/en
Priority to IL208210A priority patent/IL208210A0/en
Priority to US14/938,101 priority patent/US9587011B2/en
Priority to US15/083,584 priority patent/US9598482B2/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/08—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses
    • C07K16/10—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from viruses from RNA viruses
    • C07K16/1018—Orthomyxoviridae, e.g. influenza virus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • A61K47/6839—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting material from viruses
    • A61K47/6841—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting material from viruses the antibody targeting a RNA virus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/42—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against immunoglobulins
    • C07K16/4208—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against immunoglobulins against an idiotypic determinant on Ig
    • C07K16/4216—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against immunoglobulins against an idiotypic determinant on Ig against anti-viral Ig
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56983—Viruses
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6854—Immunoglobulins
    • G01N33/686—Anti-idiotype
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/54—F(ab')2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/55—Fab or Fab'
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622—Single chain antibody (scFv)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/005—Assays involving biological materials from specific organisms or of a specific nature from viruses
    • G01N2333/08—RNA viruses
    • G01N2333/11—Orthomyxoviridae, e.g. influenza virus
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2469/00—Immunoassays for the detection of microorganisms

Definitions

  • the present invention in general falls within the field of immunology. More specifically, the invention concerns monoclonal antibodies directed against the HA (hemagglutinin) antigen of the influenza A virus.
  • influenza virus epidemics represent an important cause of morbidity and mortality throughout the world.
  • United States of America it is estimated that more than 200,000 people are hospitalized each year for syndromes connected to influenza viruses, with about 40,000 deaths more or less directly related thereto (Thompson et al., JAMA, 2003, 289:179-186).
  • Thompson et al. JAMA, 2003, 289:179-186.
  • the only available prophylactic/therapeutic aid would be to resort to the two available classes of antiviral drugs: the M2 protein inhibitors (amantadine and rimantadine), and the neuraminidase inhibitors (osel- tamivir and zanamivir).
  • the M2 protein inhibitors amantadine and rimantadine
  • the neuraminidase inhibitors osel- tamivir and zanamivir
  • An alternative effective strategy could be based on neutralizing antibody preparations directed against critical viral proteins and capable of recognizing portions of such proteins which are shared among the different isolates of influenza viruses.
  • influenza viruses belong to the Orthomyxoviridae family and are characterized by the presence of an envelope derived from infected cell membranes, on which approximately 500 spikes are present, also referred to as projections.
  • projections consist of trimers and tetramers from two important viral surface proteins: hemagglutinin (HA) and neuraminidase (NA).
  • HA hemagglutinin
  • NA neuraminidase
  • An integral membrane protein (M2) is also found on the envelope surface, which protein is present in much lower numbers compared to hemagglutinin and neuraminidase, and also organized in tetramers.
  • influenza virus is further characterized by the presence, within the core, of a segmented genome comprised of 8 single stranded RNA fragments. Based on the features of some proteins within the virion (NP and Ml), three influenza virus types are recognizable: type A, type B, and type C.
  • Type A and type B viruses are responsible for the annual epidemics. Instead, type C viruses are responsible for less severe syndromes. Within type A viruses (the only ones responsible for pandemics and capable of causing the most severe syndromes even during annual epidemics), different subtypes are also recognizable based on the antigenic features of hemagglutinin and neuraminidase.
  • the subtypes that have affected humans in the course of recent history are subtypes HlNl and H3N2 (still circulating at present and contained in vaccine preparations), as well as subtype H2N2, no longer circulating since 1968 and responsible for the so called "Asiatic" flu in 1957.
  • Other subtypes have sporadically affected humans (H9N2, H7N7, and the so dreaded recent H5N1 subtype), but they have not succeeded in spreading effectively and displacing the circulating subtypes.
  • hemagglutinin is the protein that allows the virus to recognize the sialic acid present on the surface of some cells, and to infect them. Instead, neuraminidase operates at the end of the viral replication cycle, that is during the release of new virus particles from the infected cells. Its function is to assist the release of hemagglutinin of the newly formed virions from the sialic acid present on the surface of the cell that produced them.
  • the key role played by these two proteins, as well as their display on the virus surface explain why they represent the main target of the immune response, and why they are susceptible to a high rate of mutation.
  • the annual epidemics are caused by viruses that are more or less different from the ones of the previous years, and therefore are more or less effectively able to escape the immune response they stimulated.
  • the progressive accumulation of point mutations in hemagglutinin (mostly) and neuraminidase (secondarily) makes the protective antibodies, produced in the course of previous epidemics, on the whole progressively ineffective.
  • the main protective role within the anti-influenza immune response is played by the humoral component.
  • Antibodies exert their protective role primarily interfering with the binding of hemagglutinin to sialic acid, thereby preventing infection of the cells.
  • Such a selective pressure determines the high rate of mutation in hemagglutinin.
  • Sequence studies performed on H3 hemagglutinin subtype from 1968 through 1999 have revealed a total of 101 amino acid mutations (on a total of approximately 560 amino acids), with an average of about 3.5 mutations per year. 60% of mutations which occurred in the studied period were retained in the circulating viruses the following year too, indicative of the persistence of an immune-mediated selective pressure.
  • HOMOLOGOUS IMMUNITY related to the individual isolate. This type of immunity is always seen after an infection or a vaccination, but it provides a very limited protection against other isolates.
  • HOMOSUBTYPE IMMUNITY related to isolates belonging to the same subtype. This type of immunity is often seen after an infection or a vaccination, but is lost when the mutation rate in hemagglutinin and/or neuraminidase increases considerably.
  • HETEROSUBTYPE IMMUNITY related to isolates belonging to different subtypes. This type of immunity is extremely rare both in case of natural infection and in case of vaccination. From the strategic point of view, it is the most important immunity, as its presence and stimulation would be equivalent to the resistance to infection by every type A influenza virus.
  • mice depleted of CD8 lymphocytes are still able to display a het- erosubtype immunity, in contrast with mice depleted of the type B lymphocyte component (Nguyen HH, J Inf. Dis. 2001, 183: 368-376).
  • An even more recent study has confirmed this data, highlighting a crucial role of antibodies, even if not neutralizing, directed precisely against epitopes that are conserved among the different subtypes (Rangel-Moreno et al. The J of Immunol, 2008, 180: 454-463).
  • one object of the present invention is to provide a monoclonal antibody, preferably human or humanized, reactive against the different subtypes of the influenza A virus.
  • Another object of the present invention is to provide a monoclonal antibody, preferably human or humanized, with neutralizing activity towards multiple subtypes of the influenza A virus.
  • Such an antibody would be an effective means of prevention when administered to patients at risk. Furthermore, the use of a human or humanized monoclonal antibody for human patients would give a further advantage, as the antibody would certainly be well tolerated.
  • the monoclonal antibody with the above-mentioned features could represent a key factor for the design of innovative vaccines capable of inducing an extremely more effective, protective and broad-range immunity, compared to that induced by the currently used vaccines.
  • the present inventors have surprisingly succeeded in providing monoclonal antibodies with the above-mentioned desirable features.
  • a first object of the present invention is a monoclonal antibody directed against the hemagglutinin antigen of the influenza A virus, characterized by being able to bind multiple subtypes of the influenza A virus.
  • a second object of the present invention is a monoclonal antibody directed against the influenza A virus, characterized by having a neutralizing activity towards multiple subtypes of the influenza A virus.
  • a neutralizing monoclonal antibody recognizes influenza A virus hemagglutinin (HA) as the antigen.
  • the monoclonal antibodies of the invention are preferably human or humanized antibodies.
  • the monoclonal antibody produced by clone INF28 (designated as Fab28) represents one preferred embodiment of the invention, as the inventors have experimentally proved that this antibody displays a neutralizing activity towards multiple influenza A virus subtypes.
  • Fab28 a neutralizing activity towards multiple influenza A virus subtypes.
  • heterosubtype cross-neutralizing activity For the sake of brevity, such an immunological property will sometimes be referred to herein below as "heterosubtype cross-neutralizing activity”.
  • the Fab28 antibody is characterized by a heavy chain variable domain with the amino acid sequence SEQ ID NO: 1 and a light chain variable domain with the amino acid sequence SEQ ID NO:2.
  • the nucleotide sequence encoding for the heavy chain variable domain is SEQ ID NO: 3 and the nucleotide sequence encoding for the light chain variable domain is SEQ ID NO:4.
  • the experimental section describes the manufacture of the monoclonal anti- bodies of the invention as Fab fragments.
  • Fab fragments include whole immunoglobulins, or other kinds of antibody fragments, such as for instance F(ab') 2 fragments or antibody fragments smaller than Fabs, or peptides that have the same immunological properties as those experimentally demonstrated for the Fab of the invention.
  • Single chain antibodies can be constructed according to the method described in US patent 4,946,778 by Ladner et al., hereby included as reference.
  • Single chain antibodies comprise the light and heavy chain variable regions linked by a flexible linker.
  • the antibody fragment designated as single domain antibody is even smaller than the single chain antibody, as it comprises only one isolated VH domain. Techniques for obtaining single domain antibodies having, at least partially, the same binding ability as the whole antibody, are described in the prior art.
  • VH single domain antibody variable region of an antibody's heavy chain
  • antibody will then be used to refer to all the embodiments mentioned above, including whole immunoglobulins, Fab fragments or other antibody fragment types, single chain antibodies, single domain antibodies, etc.
  • the monoclonal antibodies of the invention may be generated and used in a free form or in a carrier-conjugated form.
  • a carrier is any molecule or chemical or biological entity capable of conjugating with an antibody and making it immunogenic or increasing its immuno- genicity.
  • Non-limiting examples of carriers are proteins such as KLH (keyhole limpet hemocyanin), edestin, thyroglobulin, albumins as bovine serum albumin (BSA) or human serum albumin (HSA), erythrocytes such as sheep erythrocytes (SRBC), tetanus anatoxin, cholera anatoxin, polyamino acids such as for example poly(D-lysine:D-glutamic acid) and the like, hi order to facilitate the binding of the antibody to the carrier, the antibody C- terminus or N-terminus may be modified, for example, by the insertion of additional amino acid residues, for instance one or more cysteine residues that are able to form disulfide bridges
  • the monoclonal antibodies of the invention are particularly suited for use in medical applications, particularly in the manufacture of a medicament for the broad-range prophylactic or therapeutic treatment of influenza A virus in- fections.
  • a monoclonal antibody of the invention preferably the antibody Fab28
  • a medicament for the prophylactic or therapeutic treatment of pathologies caused by influenza A virus infections, such as for instance the influenza syndrome is within the scope of the invention.
  • Fab28 antibody includes not only the Fab fragments but also any other form into which the antibody can be prepared, for example whole immunoglobulins, other kinds of antibody fragments, single chain antibodies, etc.
  • the monoclonal antibodies have been obtained by molecular biology techniques starting from an EBV-transformed lymphocyte capable of producing cross-reactive monoclonal antibodies, thus able to recognize MDCK cell lysates infected with the two reference isolates as referred to herein below, which belong to different subtypes of the influenza A virus: HlNl, strain A/PR/8/34 and H3N2, strain A/PC/ 1/73.
  • the specific procedures used to generate the transformed B cell lines from patients' peripheral blood are described in the experimental section.
  • the ability of the monoclonal antibodies of the invention to react with cell lysates infected with different influenza A virus subtypes were verified by ELISA and immunofluorescence.
  • a neutralizing assay was carried out in order to verify the in vitro biological activity of the antibodies.
  • the Fab28 antibody showed a heterosubtype cross-neutralizing activity towards the reference type A viral isolates as indicated above.
  • the antibodies of the invention are extremely effective in conferring a passive immunity towards the influenza A virus to the subjects to whom they are administered, and that, accordingly, they are particularly useful in the broad-range prophylactic or therapeutic treatment of influenza A virus infections or pathologies directly or indirectly caused by influenza A virus infection.
  • pathologies is the influenza syndrome.
  • hemagglutinin conformational epitope that Fab28 binds to is described in the experimental section.
  • Such a conformational epitope lies between hemagglutinin HAl region and HA2 region and includes W357 and T358 residues on HA2 region and N336, 1337 and P338 residues on HAl region.
  • the numbering of the residues is based on the hemagglutinin sequence from HlNl/A/PR/8/34 isolate in the database BLAST (SEQ ID NO: 5).
  • a further object of the invention is a pharmaceutical composition
  • a pharmaceutical composition comprising an effective amount of a monoclonal antibody of the invention as the active ingredient and a pharmaceutically acceptable carrier and/or diluent.
  • An effective amount is that which is able to induce a favourable effect in the subject to which the composition is administered, for example to neutralize the influenza A virus or interfere with the virus replication.
  • subject designates any animal host to which the composition can be administered, including humans.
  • Non-limiting examples of useful pharmaceutically acceptable carriers or diluents for the pharmaceutical composition of the invention include stabilizers such as SPGA, carbohydrates (for example, sorbitol, mannitol, starch, sucrose, glucose, dextran), proteins such as albumin or casein, protein-containing agents such as bovine serum or skimmed milk, and buffers (for example phosphate buffer).
  • stabilizers such as SPGA
  • carbohydrates for example, sorbitol, mannitol, starch, sucrose, glucose, dextran
  • proteins such as albumin or casein
  • protein-containing agents such as bovine serum or skimmed milk
  • buffers for example phosphate buffer
  • the monoclonal antibodies of the invention can also be advantageously used as diagnostic reagents in an in vitro method for the detection of anti-influenza A virus antibodies with identical or similar neutralizing properties in a biological sample previously obtained from ⁇ a patient (such as for example a serum, plasma, blood sample or any other suitable biological material).
  • Anti-influenza A virus antibodies with identical or similar neutralizing properties are antibodies that display a heterosubtype cross-neutralizing activity versus the influenza A virus. These antibodies may be found in the biological sample from the patient as a result of a previous exposure to an influenza A virus, or because the patient had been previously administered a monoclonal antibody of the invention for therapeutic or prophylactic or research purposes.
  • An assay method for detecting, in a patient's biological sample, the presence of anti- influenza A virus antibodies having a heterosubtype cross-neutralizing activity comprising contacting the said biological sample with a monoclonal antibody of the invention, as a specific assay reagent, is thus included in the scope of the invention.
  • the assay can be a qualitative or quantitative one.
  • the detection or quantification of anti- influenza A virus antibodies having a heterosubtype cross-neutralizing activity may be carried out by, for example, a competitive ELISA assay.
  • a diagnostic kit comprising a monoclonal antibody according to the invention as a specific reagent is also within the scope of the invention, the said kit being particularly designed for the detection or quantification of anti-influenza A virus antibodies having a heterosubtype cross-neutralizing activity towards the influenza A virus in a biological sample derived from a patient.
  • the monoclonal antibodies of the invention can be used as specific reagents in an assay method for detecting or quantifying, in a previously prepared immunogenic or vaccine composition, epitopes capable of evoking, in the subject to which such a composition has been administered, anti-influenza A virus antibodies having neutralizing properties identical or similar to those of the monoclonal antibody of the invention, that is a heterosubtype cross-neutralizing activity towards the influenza A virus.
  • Such a method is predicted to be useful for the assessment of any preparation to be used as a vaccine or immunogenic preparation, as the recognition by the monoclonal antibody of the invention could be indicative of the presence, in the immunogenic preparation and/or vaccine, of one or more epitopes capable of stimulating the production of antibody clones capable of recognizing an advantageous epitope, such as for example an epitope capable of eliciting a heterosubtype immunity against the influenza A virus.
  • the monoclonal antibodies of the invention may be used for the manufacture of an- ti-idiotype antibodies according to methods per se known.
  • Anti-idiotype antibodies are antibodies specifically directed towards the idiotype of the broad-range neutralizing antibodies used to prepare them, and as such are able to mimic the key epitopes they recognize.
  • anti-idiotype antibodies directed against a monoclonal antibody of the invention are also included in the scope of the invention.
  • the patients enrolled in the study were selected so as to increase the chances of cloning cross-reactive anti-influenza antibodies, that is antibodies capable of recognizing, and potentially of neutralizing, influenza virus isolates belonging to different subtypes.
  • cross-reactive anti-influenza antibodies that is antibodies capable of recognizing, and potentially of neutralizing, influenza virus isolates belonging to different subtypes.
  • influenza virus sometimes for professional reasons, as physicians, pediatricians, people working in kindergartens and schools
  • These rare individuals were thought to be less susceptible to influenza virus infection due to the development, for still unknown reasons, of an effective heterosubtype immunity. For this reason they were thought to be the best candidates for the generation of human monoclonal antibodies.
  • inclusion criteria were obeyed:
  • MDCK (Madin-Darby canine kidney) cells (ATCC® no. CCL-34TM) propagated in Modified Eagle Medium (MEM) (GIBCO), supplemented with 10% inactivated fetal bovine serum (FBS) (treatment at 56°C for 30 minutes) (EuroClone), 50 ⁇ g/ml penicillin, 100 ⁇ g/ml streptomycin (GIBCO) and 2 mM L-glutamine (EuroClone) were used as the cell line.
  • the cells were incubated at 37 0 C in a 5% CO 2 atmosphere and were passaged at a 1:3 ratio twice a week.
  • influenza virus isolates were used: HlNl, strain A/PR/8/34 (ATCC® no. VR-1469TM); H3N2, strain A/PC/1/73 (ATCC® no. VR-810), and strain B/Lee/40 (ATCC® no. VR-101).
  • MEM serum-free trypsin
  • SIGMA serum-free trypsin
  • the supernatant was collected, centrifuged at 1000 RCF (relative centrifugal force) for 10 minutes to eliminate the cell debris and filtered with 0.22 ⁇ m filters (MILLIPORE). The supernatant was then aliquoted and stored at -80°C as cell-free viruses.
  • the production of monoclonal antibodies from patients was carried out by using a transformation method via infection of B lymphocytes with Epstein-Barr virus (EBV), previously described by Cole et al, 1984 Cancer Research 22:2750-2753.
  • EBV Epstein-Barr virus
  • the supernatant from the different clones obtained was assessed for the presence of antibodies by ELISA.
  • Clones capable of producing IgG antibodies in the supernatant that are able to react in the ELISA against the cell lysates infected with the two reference isolates, subtypes HlNl and H3N2 were then selected for a subsequent characterization, hi particular, MDCK cells were infected with the aforesaid isolates at a high multiplicity of infection.
  • the cells were detached from the flask and washed twice in PBS.
  • the cell pellets were then suspended in 300 ⁇ l of lysis solution (10OmM NaCl, 10OmM Tris pH 8 and 0.5% Triton-X) and stored in ice for 20 minutes.
  • the cell debris were centrifuged away at lOOOOg for 5 minutes and the supernatant was stored at -20°C as a protein extract.
  • the preparation of the control antigen non-infected cells were treated in the same way.
  • the supernatant protein concentration was determined in duplicate using the BCATM Protein Assay Kit (Pierce).
  • sample protein dosage was determined by referring to a standard curve obtained by a series of known-concentration dilutions of bovine serum albumin (BSA). The absorbance of every sample was measured with a spectrophotometer at a wavelength of 540nm. The lysates so obtained were then used (300 ng per well) to coat an ELISA plate (COSTAR) that was incubated at 4°C overnight. The following day, the plate was washed with distilled water and blocked with PBS/1% BSA (Sigma) for 45 minutes at 37°C. Then, 40 ⁇ l of supernatant from each clone were added to each well, which were incubated for 1 hour at 37°C.
  • BSA bovine serum albumin
  • the genes encoding for the monovalent Fab chains capable of reacting with the influenza virus were cloned into a prokaryotic expression vector. This allows to avoid problems due to instability of antibody-producing cell clones, to better characterize the encoding genes from the molecular point of view, in order to have molecules that are certainly monoclonal at one's disposal, as well as increased amounts of each individual antibody.
  • the messanger RNA was extracted from the cultured clones and reverse transcribed using an oligo-dT according to methods per se known.
  • the cDNAs encoding the light chain and the Fd fragment i.e. the heavy chain portion present within the Fab fragment
  • the so obtained cDNAs were then cloned into an expression vector per se known, designated as pCb3/CAF (Burioni et al, J. Imm. Meth, 1988).
  • the gene (amplified DNA) encoding the heavy chain Fd portion of each Fab was digested with restriction enzymes Xhol and Spel (Roche) for 1.5 hours at 37°C, and subsequently inserted into the vector's cloning site for heavy chains, in turn digested with the same enzymes.
  • the light chains (amplified DNA) were digested with enzymes Sad and Xbal (Roche) and cloned into the vector similarly digested.
  • the cells were lysed by heat shock (3 freeze/thawing rounds, at -80°C and 37°C, respectively) and then centrifuged to separate the cell debris from the Fab-containing supernatant.
  • the soluble Fabs obtained were assayed by ELISA.
  • 96-Well microtiter plates (Nunc) were coated with lysates from cells infected with the above-mentioned reference virus isolates. Lysates obtained from uninfected cells were used as a negative control.
  • the ELISA plates coated with 300 ng of the lysates obtained as described were then left at 4°C overnight.
  • the plates were washed 5 times with PBS, and the unspecific binding sites were blocked with 3% albumin in PBS for 1 hour at 37°C. After removal of the blocking solution, the supernatants of the cell cultures treated as described above and containing the soluble Fabs were added thereto, followed by an incubation step at 37°C for 2 hours. After 10 washing cycles with PBS/0.05% Tween 20, 40 ⁇ l of a 1:700 dilution of a polyclonal preparation of radish peroxidase-conjugated goat anti- human Fab immunoglobulins (Sigma) in PBS/1% BSA was added thereto.
  • the substrate OPD-o- phenylenediamine
  • the substrate OPD-o- phenylenediamine
  • the plates were then incubated for 30 minutes at room temperature in the dark.
  • the reaction was quenched with IN sulfuric acid and the optical density was assessed by spectrophotometric reading at 450nm.
  • AU the assayed clones displayed reactivity towards the lysates obtained from the infected cells.
  • One bacterial clone transformed with an expression vector containing a gene pair encoding the light chain of a human antibody and the heavy chain Fd fragment was thus selected for each of the cross-reactive monoclonals.
  • Such bacterial clones are able to produce human Fabs capable of binding both the isolate A/PR/8/34 (HlNl) and the isolate A/PC/1/73 (H3N2). These clones (with the relative gene pairs) were named INF4, INF16, INF28, INF39, INF43 and INF47.
  • clones cross-reactive clones
  • Fabs cross-reactive clones
  • clones immunoafflnity purified with columns composed of a sepharose resin containing the protein G ( ⁇ 2 mg/ml), to which a polyclonal preparation of goat antibodies capable of binding human Fabs (PIERCE, Illinois) was covalently linked.
  • a single colony of each clone was inoculated into 10 ml of SB medium containing ampicillin and tetracycline at 50 ⁇ g/ml and lO ⁇ g/ml, respectively.
  • the culture which was grown overnight at 37°C, was sub-inoculated into a flask with 500 ml of SB added with the same concentration of antibiotics as before.
  • the cells subsequently induced by ImM IPTG, were left shaking overnight at 30°C.
  • the culture was centrifuged at 5000 rpm for 25 minutes and the pellet resuspended in PBS was sonicated. A further centrifuga- tion at 18,000 rpm for 25 minutes was necessary in order to remove the cell debris.
  • the supernatant was filtered, and then it was slowly passed through the above-described sepharose column.
  • the cross-reactive anti-influenza Fabs were also analyzed by an immunofluorescence assay. Briefly, the cells from the infected cultures were trypsinized and, after two washes in PBS, counted under a microscope with a hematocytometer. The cell suspension was thus used for the preparation of slides by cen- trifugation in a cytocentrifuge (Cytospin4, Shandon Southern Products) at 90 g for 3 minutes. The so prepared slides each contained a total of 2 x 10 5 cells. Control slides were prepared similarly with uninfected cells.
  • the cells were then fixed and permeabilized at room temperature with a methanol-acetone solution (used at the temperature of -20°C) for 10 minutes. After 3 washes in PBS, the cells were incubated with the different clones (100 ⁇ g/ml) for 30 minutes at 37°C in a humid chamber and subsequently washed three times in PBS. The cells were then incubated for 30 minutes at 37°C in the humid chamber in the dark with a fluoresceine isothiocyanate-conjugated goat Fab (Sigma) diluted 1 :200 in Evans Blue. The slides were examined under a fluorescence microscope (Olympus). A commercial mouse monoclonal (Argene) specific for the Ml influenza virus protein was used as a positive control.
  • TCID 50 the dose that infects 50% of the cell culture
  • TCID 50 infectivitv> 50% - 50% x dilution factor infectivity>50% - infectivity ⁇ 50%
  • the virus stock was diluted so as to use a multiplicity of infection (M.O.I.) of approximately 0.01 (1 virus particle per 100 cells) in the neutralization experiment.
  • M.O.I. multiplicity of infection
  • MDCK cells were seeded in a 24-well plate, with each well containing a sterile slide.
  • the neutralization experiment was performed on 80%-90% confluent cells, i.e. about 48 hours after the seeding thereof. Dilutions of the purified Fab fragments were then prepared, so as to attain 2.5 ⁇ g/ml, 5 ⁇ g/ml, lO ⁇ g/ml and 20 ⁇ g/ml final concentrations for each antibody.
  • Corresponding dilutions of the e509 anti- HCV antibody were prepared as a negative control.
  • the various Fab concentrations were then incubated with the same volume of diluted virus stock (M.O.I.: 0.01) for 1 hour at 37°C. 250 ⁇ l of the virus-Fab mix were subsequently added to the wells containing the cells.
  • a positive control for the infection was achieved by adding the culture medium alone to the virus stock.
  • the plate was incubated for 1 hour at 37°C in order to allow the non- neutralized virus to adsorb.
  • the inoculum was then removed and the cells were washed twice with PBS. 1.5 ml of serum-free medium with 1 ⁇ g/ml trypsin were added to each well.
  • the cell monolayer was washed with PBS and fixed with a cold methanol-acetone solution (1 :2 ratio, stored at -20°C) for 10 minutes at room temperature.
  • the fixed cells were washed and incubated with 250 ⁇ l of a commercial monoclonal anti-Mi antibody (Argene) for 30 minutes at 37 0 C in a humid chamber.
  • the cells were washed with PBS and finally incubated with a fluoresceine-conjugated goat anti- mouse antibody, diluted in Evans blue, for 30 minutes at 37°C in a humid chamber in the dark. After three washes in PBS, the slides were finally examined under a fluorescence microscope.
  • the Fabs' neutralizing activity was determined by counting the single positive cells and calculating the percentage decrease in the number of infected cells, compared to the positive control infected with the virus alone.
  • the neutralization assays were carried out in three separate sessions for each Fab. Particularly, each clone was assayed against the two different reference type A influenza strains and the reference type B strain mentioned previously. In each experiment, the different Fab dilutions were repeated in triplicate, similarly to what performed for the negative (Fab e509 anti-E2/HCV) and positive (virus and medium without Fabs) controls of infection.
  • the Fab produced by clone INF28 showed a he- terotype cross-neutralizing activity against the type A virus isolates. Instead, no reduction was detected with regard to the infecting ability of type B virus used in the study, confirming the specificity of the neutralizing activity observed, hi particular, the Fab produced by clone INF28 (called Fab 28) showed an IC 50 (the Fab concentration that inhibits 50% of infection by the virus isolate assayed) below 5 ⁇ g/ml in the case of subtype HlNl and of approximately 10 ⁇ g/ml in the case of subtype H3N2, i.e.
  • Figures 1 to 3 summarize the results obtained with Fab 28, produced by clone INF28, in the different neutralization sessions performed on the various influenza virus isolates used in the study. Particularly, Figure 1 is a graph that illustrates the neutralization percentage of the virus A/PR/8/34 (HlNl) by different Fab 28 concentrations. The results obtained with the human e509 anti-HCV Fab are reported as a negative control.
  • Figure 2 is a graph that illustrates the neutralization percentage of the virus A/PC/ 1/73 (H3N2) by different Fab 28 concentrations. The results obtained with the human e509 anti-HCV Fab are reported as a negative control.
  • Figure 3 is a graph that illustrates the neutralization percentage of the virus B/Lee/40 by different Fab 28 concentrations. The results obtained with the human e509 anti-HCV Fab are reported as a negative control.
  • the membrane was then blocked for 1 hour with 5% dried milk dissolved in IX PBS and thereafter washed three times in IX PBS - 0.1% Tween. During each wash, the membrane was left shaking on a swinging platform for 10 minutes. After which, the different Fabs, diluted in PBS with 5% dried milk, were added at the concentration of 5 ⁇ g/ml. Besides Fab 28, the following controls were added: e509 as a negative control; commercial mouse anti-HA whole IgGl (COVANCE); commercial mouse anti-Mi whole IgGl (ARGENE); mouse an- ti-M2 whole IgGl (ABCAM); human serum diluted 1:200. Each antibody was left shaking for 1 hour at room temperature.
  • COVANCE commercial mouse anti-HA whole IgGl
  • ARGENE commercial mouse anti-Mi whole IgGl
  • ABCAM mouse an- ti-M2 whole IgGl
  • the membrane was washed again in PBS as described earlier.
  • the same secondary mouse (1:1000) or human (1:2000) antibodies as described for the ELISA assay were then added, depending on the source of the antibody to be detected.
  • a working solution was prepared by mixing two substrates (SuperSignal® West Pico Chemiluminescent Substrate Pierce) in a 1 : 1 ratio, being particularly careful not to expose it to sources of light.
  • the nitrocellulose membrane was incubated for 5 minutes with the working solution and then removed and mounted in a HyperCassette (AMERSHAM). This was developed on a Kodak X-ray film in the dark room after the necessary exposure time.
  • the described assay was performed in two different sessions, and in each of them the membrane portion incubated with Fab 28 showed the presence of a band weighing slightly less than 80 KDa, consistent with the weight of the immature form of the viral hemagglutinin (HAO). This was confirmed by the same band being also displayed on the strip incubated with the anti-hemagglutinin control antibody. An analogous band, more intense than the others, was also detected in the membrane portion incubated with human serum. The result of this experiment shows that the antibody is directed against the influenza virus hemagglutinin, perfectly consistent with the neutralization data, since hemagglutinin is known to be the target of the immune neutralizing antibody response.
  • Neutralization assays were carried out by using the plaque assay technique to assess more accurately the neutralizing activity of Fab 28. Firstly, preparations of virus isolates, subtypes HlNl and H3N2, were quantified by plaque assay with the following protocol. MDCK cells were cultured in six-well plates (Costar) in MEM medium supplemented with penicillin and streptomycin (pen/strep), and enriched with 10% fetal bovine serum (FBS). After the cell monolayer had reached 100% confluence, the wells were washed with PBS and fresh MEM culture medium supplemented with the same antibiotics (pen/strep) and trypsin (1 ⁇ g/ml) was added thereto.
  • pen/strep penicillin and streptomycin
  • FBS fetal bovine serum
  • a neutralization mix was thus prepared, which comprised the virus (100 TCID50 per well) and different concentrations of the Fabs that were used (Fab 28 and control Fab).
  • the assay was performed by testing different concentrations of Fabs (20, 10, 5 and 2.5 ⁇ g/ml) against 100 TCID 50 of the diverse influenza virus strains. The virus/Fab mixtures were then incubated for 1 hour at 34°C under a 5% CO 2 atmosphere.
  • the pre-incubated preparations were transferred into the wells having a 100% confluent cell monolayer, then were incubated for 1 hour at 34°C under a 5% CO 2 atmosphere.
  • the assay was carried out and interpreted as described previously, by comparing the number of plaques obtained in the presence of Fab 28 with those obtained in the presence of the same concentration of the control Fab.
  • the assays were performed using the following influenza isolates belonging to subtypes
  • Fab 28 resulted capable of recognizing the protein only in Western blot assays performed under semi-native conditions (0.1% SDS). The same experiments had also pointed out the ability of Fab in recognizing only the immature form of the protein (HAO), but not the individual subunits (HAl and HA2). Hemagglutination inhibition assays (HAI) had been carried out in parallel, with both chicken erythrocytes and human erythrocytes. Despite the remarkable neutralizing activity, Fab 28 proved to have no HAI activity, suggesting that it did not bind residues implicated in the binding between hemagglutinin and sialic acid.
  • HAI Hemagglutination inhibition assays
  • the epitope is localized on the stem region of hemagglutinin, that is in a portion between regions HAl and HA2 (data perfectly consistent with the results achieved in the Western Blot and HAI assays).
  • the residues critical for the binding which were identified are the following: W357 and T358 on region HA2; N336; 1337; P338 on region HAl (the numbering of the residues refers to the hemagglutinin sequence from the isolate H1N1/A/PR/8/34 present in the BLAST database) (SEQ ID N0:5).
  • the assay by the escape mutants was carried out by serial infections of MDCK cells with 100 TCID50 of HlNl/A/PR/8/34 virus in the presence of 10 ⁇ g/ml of Fab 28, i.e. a Fab concentration equivalent to its IC90 against the isolate in question. Only after numerous passages, it was possible to detect infection of the cells in the presence of the Fab, indicative of a mutation occurred in the virus genome. In fact, escape mutants mutated in two residues of region HA2, 1361 and D362, were selected, which are adjacent to the region identified by the in silico approach, confirming the hypothesis that this is the region recognized by Fab 28.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Virology (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Physics & Mathematics (AREA)
  • Communicable Diseases (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Plant Pathology (AREA)
  • Epidemiology (AREA)
  • Analytical Chemistry (AREA)
  • Food Science & Technology (AREA)
  • Cell Biology (AREA)
  • Pathology (AREA)
  • General Physics & Mathematics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
PCT/IB2009/051068 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes WO2009115972A1 (en)

Priority Applications (17)

Application Number Priority Date Filing Date Title
NZ588238A NZ588238A (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes
PL09722394T PL2274335T3 (pl) 2008-03-17 2009-03-16 Przeciwciała monoklonalne zdolne do reagowania z wieloma podtypami wirusa grupy typu A
BRPI0909123A BRPI0909123B8 (pt) 2008-03-17 2009-03-16 anticorpos monoclonais, vetor de expressão, célula hospedeira, composição farmacêutica, uso do referido anticorpo, kit de diagnóstico e métodos de ensaio para detectar a presença de epítopos de vírus de influenza a
JP2011500336A JP5542118B2 (ja) 2008-03-17 2009-03-16 インフルエンザａ型ウイルスの複数のサブタイプと反応することができるモノクローナル抗体
EA201071087A EA027069B1 (ru) 2008-03-17 2009-03-16 Моноклональные антитела, способные взаимодействовать с множеством подтипов вируса гриппа а
CA2718923A CA2718923C (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes
CN200980117842.2A CN102037013B (zh) 2008-03-17 2009-03-16 能与复数个甲型流感病毒亚型反应的单克隆抗体
MX2010010120A MX2010010120A (es) 2008-03-17 2009-03-16 Anticuerpos monoclonales capaces de reaccionar con una pluralidad de subtipos del virus de la influenza a.
DK09722394.5T DK2274335T3 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a large number of influenza virus A subtypes
ES09722394T ES2544968T5 (es) 2008-03-17 2009-03-16 Anticuerpos monoclonales capaces de reaccionar con una pluralidad de subtipos del virus de la influenza A
AU2009227567A AU2009227567B2 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US12/922,850 US9200063B2 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
EP09722394.5A EP2274335B2 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes
ZA2010/06934A ZA201006934B (en) 2008-03-17 2010-08-29 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes
IL208210A IL208210A0 (en) 2008-03-17 2010-09-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes
US14/938,101 US9587011B2 (en) 2008-03-17 2015-11-11 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US15/083,584 US9598482B2 (en) 2008-03-17 2016-03-29 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITTO2008A000204 2008-03-17
IT000204A ITTO20080204A1 (it) 2008-03-17 2008-03-17 Anticorpi monoclonali atti a reagire con una pluralita di sottotipi del virus influenzale a

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/922,850 A-371-Of-International US9200063B2 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US14/938,101 Division US9587011B2 (en) 2008-03-17 2015-11-11 Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes

Publications (1)

Publication Number Publication Date
WO2009115972A1 true WO2009115972A1 (en) 2009-09-24

Family

ID=40293277

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2009/051068 WO2009115972A1 (en) 2008-03-17 2009-03-16 Monoclonal antibodies capable of reacting with a plurality of influenza virus a subtypes

Country Status (22)

Country Link
US (3) US9200063B2 (es)
EP (1) EP2274335B2 (es)
JP (1) JP5542118B2 (es)
KR (1) KR101605573B1 (es)
CN (1) CN102037013B (es)
AU (1) AU2009227567B2 (es)
BR (1) BRPI0909123B8 (es)
CA (1) CA2718923C (es)
DK (1) DK2274335T3 (es)
EA (1) EA027069B1 (es)
ES (1) ES2544968T5 (es)
HU (1) HUE025329T2 (es)
IL (1) IL208210A0 (es)
IT (1) ITTO20080204A1 (es)
MX (1) MX2010010120A (es)
MY (1) MY157359A (es)
NZ (1) NZ588238A (es)
PL (1) PL2274335T3 (es)
PT (1) PT2274335E (es)
SG (1) SG188890A1 (es)
WO (1) WO2009115972A1 (es)
ZA (1) ZA201006934B (es)

Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ITTO20090414A1 (it) * 2009-06-01 2010-12-02 Pomona Biotechnologies Llc Anticorpi monoclonali come medicamento per il trattamento terapeutico e/o profilattico delle infezioni da virus influenzale a (h1n1) di origine suina (s-oiv)
ITTO20100237A1 (it) * 2010-03-26 2011-09-27 Pomona Biotechnologies Llc Immunoglobuline intere della classe delle igg per l'uso come medicamento antinfluenzale
WO2011117848A1 (en) * 2010-03-26 2011-09-29 Pomona Ricerca S.R.L. Full-length immunoglobulins of the igg isotvpe capable of recognizing a heterosubtvpe neutralizing epitope on the hemagglutinin stem region and their use as anti-influenza medicament
ITTO20110067A1 (it) * 2011-01-26 2012-07-27 Pomona Ricerca Srl Immunoglobuline intere di isotipo igg atte a riconoscere un epitopo di neutralizzazione eterosubtipica sulla regione stelo (stem region) dell'emoagglutinina e loro uso come medicamento antinfluenzale
EP2486054A2 (en) * 2009-10-09 2012-08-15 Emory University Recombinant antibodies against h1n1 influenza
WO2012145572A1 (en) 2011-04-20 2012-10-26 The Trustees Of The University Of Pennsylvania Regimens and compositions for aav-mediated passive immunization of airborne pathogens
US8367061B2 (en) 2007-01-30 2013-02-05 Pomona Ricera S.R.L. Anti-idiotype monoclonal antibodies mimicking the HIV gp120 CD4-binding (CD4bs)
WO2013081463A2 (en) 2011-12-02 2013-06-06 Aimm Therapeutics B.V. Influenza a virus specific antibodies
US8470327B2 (en) 2009-05-11 2013-06-25 Crucell Holland B.V. Human binding molecules capable of neutralizing influenza virus H3N2 and uses thereof
EP2626425A1 (en) * 2010-09-03 2013-08-14 Fujita Health University Influenza virus neutralizing antibody and method for screening same
US8623363B2 (en) 2008-12-22 2014-01-07 Pomona Ricerca S.R.L. Anti-HCV monoclonal antibody as a medicament for the therapeutic treatment and prevention of HCV infections
WO2014078268A2 (en) 2012-11-13 2014-05-22 Genentech, Inc. Anti-hemagglutinin antibodies and methods of use
US8877200B2 (en) 2012-05-10 2014-11-04 Visterra, Inc. HA binding agents
EP2294084B1 (en) 2008-05-27 2015-09-09 Pomona Ricerca S.r.l. Monoclonal antibodies having homosubtype cross -neutralization properties against influenza a viruses subtype h1
US9200063B2 (en) 2008-03-17 2015-12-01 Pomona Ricerca S.R.L. Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US9321829B2 (en) 2011-10-18 2016-04-26 Emory University Antibodies directed against influenza
US9340603B2 (en) 2008-07-25 2016-05-17 Institute For Research In Biomedicine Neutralizing anti-influenza A virus antibodies and uses thereof
US9587010B2 (en) 2011-07-18 2017-03-07 The Institute For Research In Biomedicine Neutralizing anti-influenza A virus antibodies and uses thereof
US9951122B2 (en) 2007-12-06 2018-04-24 Dana-Farber Cancer Institute, Inc. Antibodies against influenza virus and methods of use thereof
WO2018160573A1 (en) 2017-02-28 2018-09-07 The Trustees Of The University Of Pennsylvania Influenza vaccines based on aav vectors
US10138295B2 (en) 2014-05-13 2018-11-27 The Trustees Of The University Of Pennsylvania Compositions comprising AAV expressing dual antibody constructs and uses thereof
US10294292B2 (en) 2014-07-15 2019-05-21 Medimmune, Llc Neutralizing anti-influenza B antibodies and uses thereof
US10442854B2 (en) 2015-06-01 2019-10-15 Medimmune, Llc Neutralizing anti-influenza binding molecules and uses thereof
US10494419B2 (en) 2013-10-02 2019-12-03 Medimmune, Llc Neutralizing anti-influenza A antibodies and uses thereof
US10513553B2 (en) 2015-11-13 2019-12-24 Visterra, Inc. Compositions and methods for treating and preventing influenza
US11230593B2 (en) 2019-03-25 2022-01-25 Visterra, Inc. Compositions and methods for treating and preventing influenza
WO2022119871A2 (en) 2020-12-01 2022-06-09 The Trustees Of The University Of Pennsylvania Novel compositions with tissue-specific targeting motifs and compositions containing same
WO2022232289A1 (en) 2021-04-27 2022-11-03 Generation Bio Co. Non-viral dna vectors expressing therapeutic antibodies and uses thereof
US11535665B2 (en) 2015-05-13 2022-12-27 The Trustees Of The University Of Pennsylvania AAV-mediated expression of anti-influenza antibodies and methods of use thereof
US11547756B2 (en) 2016-01-13 2023-01-10 Medimmune, Llc Method of treating influenza A
US11578341B2 (en) 2017-02-28 2023-02-14 The Trustees Of The University Of Pennsylvania Compositions useful in treatment of spinal muscular atrophy
WO2023177655A1 (en) 2022-03-14 2023-09-21 Generation Bio Co. Heterologous prime boost vaccine compositions and methods of use
US11827906B2 (en) 2017-02-28 2023-11-28 The Trustees Of The University Of Pennsylvania Adeno-associated virus (AAV) clade f vector and uses therefor

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012521786A (ja) 2009-03-30 2012-09-20 モウント シナイ スクール オフ メディシネ インフルエンザウイルスワクチン及びその使用
KR20120132506A (ko) 2010-02-18 2012-12-05 마운트 시나이 스쿨 오브 메디슨 인플루엔자 바이러스 질환의 예방 및 치료에 사용되는 백신
WO2011123495A1 (en) 2010-03-30 2011-10-06 Mount Sinai School Of Medicine Influenza virus vaccines and uses thereof
CN102775469B (zh) * 2011-05-12 2018-02-09 厦门大学 甲型流感病毒核衣壳蛋白的抗原表位及其用途
US10131695B2 (en) 2011-09-20 2018-11-20 Icahn School Of Medicine At Mount Sinai Influenza virus vaccines and uses thereof
CA2895508A1 (en) 2012-12-18 2014-06-26 Icahn School Of Medicine At Mount Sinai Influenza virus vaccines and uses thereof
WO2014159960A1 (en) 2013-03-14 2014-10-02 Icahn School Of Medicine At Mount Sinai Antibodies against influenza virus hemagglutinin and uses thereof
TWI701258B (zh) 2014-12-19 2020-08-11 美商再生元醫藥公司 流行性感冒病毒血球凝集素之人類抗體
JP2018504412A (ja) 2015-01-23 2018-02-15 アイカーン スクール オブ メディシン アット マウント サイナイ インフルエンザウイルスワクチン接種レジメン
US11266734B2 (en) 2016-06-15 2022-03-08 Icahn School Of Medicine At Mount Sinai Influenza virus hemagglutinin proteins and uses thereof
CA3058652A1 (en) 2017-04-07 2018-10-11 Icahn School Of Medicine At Mount Sinai Anti-influenza b virus neuraminidase antibodies and uses thereof
EP3802571A4 (en) * 2018-06-11 2022-03-02 GlaxoSmithKline Consumer Healthcare Holdings (US) LLC PAIRS OF ANTIBODY FOR USE IN A RAPID INFLUENZA A DIAGNOSTIC TEST
KR20200060969A (ko) * 2018-11-23 2020-06-02 (주)셀트리온 인플루엔자 바이러스 질환을 치료하기 위한 투여 요법
CN115724952B (zh) * 2022-07-13 2023-10-31 扬州大学 一种靶向甲型流感病毒保守线性b细胞表位的广谱单克隆抗体及其应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0675199A2 (en) * 1994-03-30 1995-10-04 Takara Shuzo Co. Ltd. A DNA which codes for the variable region of the anti-human influenza A type virus antibody recognizing the H,N, and H2N2 subtypes of haemagglutinin
WO2002046235A1 (fr) * 2000-12-07 2002-06-13 Technopharm Anticorps monoclonal humain dirige contre le virus influenza ou un fragment de celui-ci
WO2007134327A2 (en) * 2006-05-15 2007-11-22 Sea Lane Biotechnologies, Llc. Neutralizing antibodies to influenza viruses

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA836080B (en) 1982-08-23 1984-04-25 Scripps Clinic Res Broad spectrum influenza antisera
US4946778A (en) 1987-09-21 1990-08-07 Genex Corporation Single polypeptide chain binding molecules
US6812024B2 (en) 1987-03-16 2004-11-02 Mcgready Roland Keith Anti-paratopic antibody as an immunogen
US5245015A (en) 1991-04-26 1993-09-14 Tanox Biosystems, Inc. Monoclonal antibodies which neutralize HIV-1 through reaction with a conformational epitope in vitro
WO1992015885A1 (en) 1991-03-11 1992-09-17 Idec Pharmaceuticals Corporation Methods for selecting antibody reagents; anti-idiotype antibodies; and aids vaccine formulations
CA2131692A1 (en) 1992-03-09 1993-09-16 Sybille Muller An anti-idiotypic antibody and its use in diagnosis and therapy in hiv-related disease
EP0621339B1 (en) 1992-09-17 2001-10-24 Takara Shuzo Co. Ltd. Immunogenic human influenza A virus haemagglutinin polypeptides
GB9221654D0 (en) * 1992-10-15 1992-11-25 Scotgen Ltd Recombinant human anti-cytomegalovirus antibodies
US6057421A (en) 1994-11-30 2000-05-02 Immpheron, Inc. Variable heavy and light chain regions of murine monoclonal antibody 1F7
CN1325517C (zh) 1998-07-21 2007-07-11 展马博联合股份有限公司 抗丙型肝炎病毒抗体及其用途
JP2004524829A (ja) 2000-12-01 2004-08-19 アメリカ合衆国 Ｃ型肝炎ウイルスのｅ２糖タンパク質に特異的なモノクローナル抗体、ならびにｃ型肝炎の診断、治療、および予防におけるそれらの使用
US6768004B2 (en) 2001-01-11 2004-07-27 Mueller Sybille Nucleotide sequences encoding variable regions of heavy and light chains of monoclonal antibody 1F7, an anti-idiotypic antibody reactive with anti-HIV antibodies
US6964199B2 (en) 2001-11-02 2005-11-15 Cantocor, Inc. Methods and compositions for enhanced protein expression and/or growth of cultured cells using co-transcription of a Bcl2 encoding nucleic acid
US7625566B2 (en) 2002-01-17 2009-12-01 Polymun Scientific Immunbiologische Forschung Gmbh Anti-idiotypic monoclonal antibody reactive with HIV neutralizing antibody 2F5
ITRM20020049A1 (it) 2002-01-30 2003-07-30 Biostrands S R L Frammenti fab di anticorpi monoclonali umani diretti contro la glicoproteina e2 di hcv e dotati di potere neutralizzante in vitro.
EP2450377A1 (en) 2006-09-07 2012-05-09 Crucell Holland B.V. Human binding molecules capable of neutralizing influenza virus H5N1 and uses thereof
JP2010503668A (ja) 2006-09-15 2010-02-04 フラウンホーファー ユーエスエー， インコーポレイテッド インフルエンザ抗体、組成物、および関連する方法
ITTO20070066A1 (it) 2007-01-30 2008-07-31 Pomona Biotechnologies Llc Anticorpi monoclonali anti-idiotipo mimotopi dell'antigene gp 120 di hiv
US20100316563A1 (en) 2007-09-20 2010-12-16 Bracco Imaging S.P.A. Method For The Preparation Of New Oligoclonal Antibodies
ITTO20080204A1 (it) 2008-03-17 2009-09-18 Pomona Biotechnologies Llc Anticorpi monoclonali atti a reagire con una pluralita di sottotipi del virus influenzale a
ITTO20080398A1 (it) 2008-05-27 2009-11-28 Pomona Biotechnologies Llc Anticorpi monoclonali aventi proprieta' di cross-neutralizzazione omosubtipica per virus influenzali di tipo a sottotipo h1
ITTO20080964A1 (it) 2008-12-22 2010-06-23 Natimab Therapeutics S R L Anticorpo monoclonale anti-hcv come medicamento per il trattamento terapeutico e la prevenzione di infezioni da hcv
IT1395961B1 (it) 2009-06-01 2012-11-02 Pomona Biotechnologies Llc Anticorpi monoclonali come medicamento per il trattamento terapeutico e/o profilattico delle infezioni da virus influenzale a (h1n1) di origine suina (s-oiv)
CN102958539B (zh) 2010-03-26 2015-07-01 泼莫纳搜索有限公司 能够识别血凝素干区上的杂亚型中和表位的IgG同种型全长免疫球蛋白和其作为抗-流感药物的应用

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0675199A2 (en) * 1994-03-30 1995-10-04 Takara Shuzo Co. Ltd. A DNA which codes for the variable region of the anti-human influenza A type virus antibody recognizing the H,N, and H2N2 subtypes of haemagglutinin
WO2002046235A1 (fr) * 2000-12-07 2002-06-13 Technopharm Anticorps monoclonal humain dirige contre le virus influenza ou un fragment de celui-ci
WO2007134327A2 (en) * 2006-05-15 2007-11-22 Sea Lane Biotechnologies, Llc. Neutralizing antibodies to influenza viruses

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
M. THROSBY ET AL.: "Heterosubtypic neutralizing monoclonal antibodies cross-protective against H5N1 and H1N1 recovered from human IgM+ memory B cells.", PLOS ONE, vol. 3, no. 12(e3942), 16 December 2008 (2008-12-16), U.S.A., pages 1 - 15, XP002541925 *
T. ZIEGLER ET AL.: "Type- and subtype-specific detection of influenza viruses in clinical specimens by rapid culture assay.", JOURNAL OF CLINICAL MICROBIOLOGY, vol. 33, no. 2, February 1995 (1995-02-01), pages 318 - 321, XP002541924 *
Y. SMIRNOV ET AL.: "An epitope shared by the hemagglutinins of H1, H2, H5, and H6 subtypes of influenza A virus.", ACTA VIROLOGICA, vol. 43, no. 4, 1 August 1999 (1999-08-01), Prague, pages 237 - 244, XP009095964 *
Y. SMIRNOV ET AL.: "Prevention and treatment of bronchopneumonia in mice caused by mouse-adapted variant of avian H5N2 influenza A virus using a monoclonal antibody against conserved epitope in the HA stem region.", ARCHIVES OF VIROLOGY, vol. 145, no. 8, January 2000 (2000-01-01), Vienna, pages 1733 - 1741, XP002473326 *

Cited By (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8367061B2 (en) 2007-01-30 2013-02-05 Pomona Ricera S.R.L. Anti-idiotype monoclonal antibodies mimicking the HIV gp120 CD4-binding (CD4bs)
US9951122B2 (en) 2007-12-06 2018-04-24 Dana-Farber Cancer Institute, Inc. Antibodies against influenza virus and methods of use thereof
US9587011B2 (en) 2008-03-17 2017-03-07 Pomona Ricerca S.R.L. Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US9200063B2 (en) 2008-03-17 2015-12-01 Pomona Ricerca S.R.L. Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
EP2294084B1 (en) 2008-05-27 2015-09-09 Pomona Ricerca S.r.l. Monoclonal antibodies having homosubtype cross -neutralization properties against influenza a viruses subtype h1
EP2294084B2 (en) † 2008-05-27 2018-09-05 Pomona Ricerca S.r.l. Monoclonal antibodies having homosubtype cross -neutralization properties against influenza a viruses subtype h1
US9243054B2 (en) 2008-05-27 2016-01-26 Pomona Ricerca S.R.L. Monoclonal antibodies having homosubtype cross-neutralization properties against influenza A viruses subtype H1
US9340603B2 (en) 2008-07-25 2016-05-17 Institute For Research In Biomedicine Neutralizing anti-influenza A virus antibodies and uses thereof
US8623363B2 (en) 2008-12-22 2014-01-07 Pomona Ricerca S.R.L. Anti-HCV monoclonal antibody as a medicament for the therapeutic treatment and prevention of HCV infections
US8470327B2 (en) 2009-05-11 2013-06-25 Crucell Holland B.V. Human binding molecules capable of neutralizing influenza virus H3N2 and uses thereof
US9611317B2 (en) 2009-05-11 2017-04-04 Crucell Holland B.V. Human binding molecules capable of neutralizing influenza virus H3N2 and uses thereof
US8486406B2 (en) 2009-06-01 2013-07-16 Pomona Ricerca S.R.L. Monoclonal antibodies as a medicament for the therapeutic and/or prophylactic treatment of swine-origin influenza A (H1N1) virus (S-OIV) infections
WO2010140114A1 (en) * 2009-06-01 2010-12-09 Pomona Biotechnologies Llc Monoclonal antibodies as a medicament for the therapeutic and/or prophylactic treatment of swine -origin influenza a (h1n1) virus (s-oiv) infections
ITTO20090414A1 (it) * 2009-06-01 2010-12-02 Pomona Biotechnologies Llc Anticorpi monoclonali come medicamento per il trattamento terapeutico e/o profilattico delle infezioni da virus influenzale a (h1n1) di origine suina (s-oiv)
US9458226B2 (en) 2009-10-09 2016-10-04 Emory University Recombinant antibodies against H1N1 influenza
EP2486054A4 (en) * 2009-10-09 2013-09-11 Univ Emory RECOMBINANT ANTIBODIES AGAINST H1N1 INFLUENZA
EP2486054A2 (en) * 2009-10-09 2012-08-15 Emory University Recombinant antibodies against h1n1 influenza
CN102958539A (zh) * 2010-03-26 2013-03-06 泼莫纳搜索有限公司 能够识别血凝素干区上的杂亚型中和表位的IgG同种型全长免疫球蛋白和其作为抗-流感药物的应用
EA029198B1 (ru) * 2010-03-26 2018-02-28 Помона Ричерка С.Р.Л. Полноразмерные иммуноглобулины изотипа igg, способные к распознаванию нейтрализующего эпитопа в области стебля гемагглютинина различных подтипов и их использование в качестве лекарственного средства против гриппа
US20130022608A1 (en) * 2010-03-26 2013-01-24 Pomona Ricerca S.R.L. FULL-LENGTH IgG IMMUNOGLOBULINS CAPABLE OF RECOGNIZING A HETEROSUBTYPE NEUTRALIZING EPITOPE ON THE HEMAGGLUTININ STEM REGION AND USES THEREOF
WO2011117848A1 (en) * 2010-03-26 2011-09-29 Pomona Ricerca S.R.L. Full-length immunoglobulins of the igg isotvpe capable of recognizing a heterosubtvpe neutralizing epitope on the hemagglutinin stem region and their use as anti-influenza medicament
ITTO20100237A1 (it) * 2010-03-26 2011-09-27 Pomona Biotechnologies Llc Immunoglobuline intere della classe delle igg per l'uso come medicamento antinfluenzale
CN102958539B (zh) * 2010-03-26 2015-07-01 泼莫纳搜索有限公司 能够识别血凝素干区上的杂亚型中和表位的IgG同种型全长免疫球蛋白和其作为抗-流感药物的应用
EP2626425A4 (en) * 2010-09-03 2014-02-19 Univ Fujita Health NEUTRALIZING ANTIBODIES OF THE INFLUENZA VIRUS AND ITS SCREENING METHOD
EP2626425A1 (en) * 2010-09-03 2013-08-14 Fujita Health University Influenza virus neutralizing antibody and method for screening same
US9605053B2 (en) 2010-09-03 2017-03-28 Fujita Health University Influenza virus-neutralizing antibody and screening method therefor
CN103476929A (zh) * 2010-09-03 2013-12-25 学校法人藤田学园 抗流感病毒中和抗体及其筛选方法
US9534042B2 (en) 2010-09-03 2017-01-03 Fujita Health University Influenza virus-neutralizing antibody and screening method therefor
ITTO20110067A1 (it) * 2011-01-26 2012-07-27 Pomona Ricerca Srl Immunoglobuline intere di isotipo igg atte a riconoscere un epitopo di neutralizzazione eterosubtipica sulla regione stelo (stem region) dell'emoagglutinina e loro uso come medicamento antinfluenzale
EP3699286A1 (en) 2011-04-20 2020-08-26 The Trustees of the University of Pennsylvania Regimens and compositions for aav-mediated passive immunization of airborne pathogens
WO2012145572A1 (en) 2011-04-20 2012-10-26 The Trustees Of The University Of Pennsylvania Regimens and compositions for aav-mediated passive immunization of airborne pathogens
US9587010B2 (en) 2011-07-18 2017-03-07 The Institute For Research In Biomedicine Neutralizing anti-influenza A virus antibodies and uses thereof
US10815294B2 (en) 2011-07-18 2020-10-27 Institute For Research In Biomedicine Neutralizing anti-influenza A virus antibodies and uses thereof
US10208107B2 (en) 2011-10-18 2019-02-19 Emory University Antibodies directed against influenza
US9321829B2 (en) 2011-10-18 2016-04-26 Emory University Antibodies directed against influenza
WO2013081463A2 (en) 2011-12-02 2013-06-06 Aimm Therapeutics B.V. Influenza a virus specific antibodies
WO2013081463A3 (en) * 2011-12-02 2013-11-14 Aimm Therapeutics B.V. Influenza a virus specific antibodies
US9718874B2 (en) 2011-12-02 2017-08-01 Aimm Therapeutics B.V. Influenza A virus specific antibodies
AU2012346669B2 (en) * 2011-12-02 2017-08-31 Kling Biotherapeutics B.V. Influenza A virus specific antibodies
US8877200B2 (en) 2012-05-10 2014-11-04 Visterra, Inc. HA binding agents
US12024552B2 (en) 2012-05-10 2024-07-02 Visterra, Inc. Ha binding agents
US10800835B2 (en) 2012-05-10 2020-10-13 Visterra, Inc. HA binding agents
US9969794B2 (en) 2012-05-10 2018-05-15 Visterra, Inc. HA binding agents
US9096657B2 (en) 2012-05-10 2015-08-04 Visterra, Inc. HA binding agents
US9284365B2 (en) 2012-11-13 2016-03-15 Genentech, Inc. Anti-hemagglutinin antibodies and methods of use
US9067979B2 (en) 2012-11-13 2015-06-30 Genentech, Inc. Anti-hemagglutinin antibodies and methods of use
EP3461501A1 (en) 2012-11-13 2019-04-03 F. Hoffmann-La Roche AG Anti-hemagglutinin antibodies and methods of use
US9908931B2 (en) 2012-11-13 2018-03-06 Genentech, Inc. Anti-hemagglutinin antibodies and methods of use
WO2014078268A2 (en) 2012-11-13 2014-05-22 Genentech, Inc. Anti-hemagglutinin antibodies and methods of use
US9598481B2 (en) 2012-11-13 2017-03-21 Genetech, Inc. Anti-hemagglutinin antibodies and methods of use
US11932682B2 (en) 2013-10-02 2024-03-19 Medimmune, Llc Neutralizing anti-influenza A antibodies and uses thereof
US11186627B2 (en) 2013-10-02 2021-11-30 Medimmune, Llc Neutralizing anti-influenza A antibodies and uses thereof
US10494419B2 (en) 2013-10-02 2019-12-03 Medimmune, Llc Neutralizing anti-influenza A antibodies and uses thereof
US10385119B2 (en) 2014-05-13 2019-08-20 Trustees Of The University Of Pennsylvania Compositions comprising AAV expressing dual antibody constructs and uses thereof
US10138295B2 (en) 2014-05-13 2018-11-27 The Trustees Of The University Of Pennsylvania Compositions comprising AAV expressing dual antibody constructs and uses thereof
US10647758B2 (en) 2014-05-13 2020-05-12 The Trustees Of The University Of Pennsylvania Compositions comprising AAV expressing dual antibody constructs and uses thereof
US10975140B2 (en) 2014-05-13 2021-04-13 The Trustees Of The University Of Pennsylvania Compositions comprising AAV expressing dual antibody constructs and uses thereof
US10294292B2 (en) 2014-07-15 2019-05-21 Medimmune, Llc Neutralizing anti-influenza B antibodies and uses thereof
US10519221B2 (en) 2014-07-15 2019-12-31 Medimmune, Llc Neutralizing anti-influenza B antibodies and uses thereof
US11787853B2 (en) 2014-07-15 2023-10-17 Medimmune, Llc Neutralizing anti-influenza b antibodies and uses thereof
US11174304B2 (en) 2014-07-15 2021-11-16 Medimmune, Llc Neutralizing anti-influenza B antibodies and uses thereof
US11535665B2 (en) 2015-05-13 2022-12-27 The Trustees Of The University Of Pennsylvania AAV-mediated expression of anti-influenza antibodies and methods of use thereof
US11926657B2 (en) 2015-06-01 2024-03-12 Medimmune, Llc Neutralizing anti-influenza binding molecules and uses thereof
US10882897B2 (en) 2015-06-01 2021-01-05 Medimmune, Llc Neutralizing anti-influenza binding molecules and uses thereof
US10442854B2 (en) 2015-06-01 2019-10-15 Medimmune, Llc Neutralizing anti-influenza binding molecules and uses thereof
US11524993B2 (en) 2015-06-01 2022-12-13 Medimmune, Llc Neutralizing anti-influenza binding molecules and uses thereof
US10513553B2 (en) 2015-11-13 2019-12-24 Visterra, Inc. Compositions and methods for treating and preventing influenza
US11547756B2 (en) 2016-01-13 2023-01-10 Medimmune, Llc Method of treating influenza A
US11578341B2 (en) 2017-02-28 2023-02-14 The Trustees Of The University Of Pennsylvania Compositions useful in treatment of spinal muscular atrophy
US11827906B2 (en) 2017-02-28 2023-11-28 The Trustees Of The University Of Pennsylvania Adeno-associated virus (AAV) clade f vector and uses therefor
US10786568B2 (en) 2017-02-28 2020-09-29 The Trustees Of The University Of Pennsylvania AAV mediated influenza vaccines
WO2018160573A1 (en) 2017-02-28 2018-09-07 The Trustees Of The University Of Pennsylvania Influenza vaccines based on aav vectors
US11230593B2 (en) 2019-03-25 2022-01-25 Visterra, Inc. Compositions and methods for treating and preventing influenza
WO2022119871A2 (en) 2020-12-01 2022-06-09 The Trustees Of The University Of Pennsylvania Novel compositions with tissue-specific targeting motifs and compositions containing same
WO2022232289A1 (en) 2021-04-27 2022-11-03 Generation Bio Co. Non-viral dna vectors expressing therapeutic antibodies and uses thereof
WO2023177655A1 (en) 2022-03-14 2023-09-21 Generation Bio Co. Heterologous prime boost vaccine compositions and methods of use

Also Published As

Publication number Publication date
MY157359A (en) 2016-05-31
ES2544968T5 (es) 2022-11-22
US20160200801A1 (en) 2016-07-14
JP5542118B2 (ja) 2014-07-09
SG188890A1 (en) 2013-04-30
JP2011517403A (ja) 2011-06-09
EP2274335B2 (en) 2022-07-27
HUE025329T2 (en) 2016-02-29
IL208210A0 (en) 2010-12-30
ZA201006934B (en) 2011-12-28
CA2718923A1 (en) 2009-09-24
CA2718923C (en) 2020-07-07
EP2274335B8 (en) 2015-06-17
US9598482B2 (en) 2017-03-21
US20160060325A1 (en) 2016-03-03
NZ588238A (en) 2012-08-31
PT2274335E (pt) 2015-09-18
ES2544968T3 (es) 2015-09-07
EA201071087A1 (ru) 2011-04-29
CN102037013A (zh) 2011-04-27
KR101605573B1 (ko) 2016-03-22
CN102037013B (zh) 2015-01-28
BRPI0909123A2 (pt) 2019-02-26
AU2009227567B2 (en) 2014-06-26
AU2009227567A1 (en) 2009-09-24
EA027069B1 (ru) 2017-06-30
MX2010010120A (es) 2010-12-02
EP2274335B1 (en) 2015-05-13
US9200063B2 (en) 2015-12-01
KR20100126810A (ko) 2010-12-02
PL2274335T3 (pl) 2015-10-30
BRPI0909123B1 (pt) 2020-12-01
BRPI0909123B8 (pt) 2021-06-01
US20110014187A1 (en) 2011-01-20
ITTO20080204A1 (it) 2009-09-18
EP2274335A1 (en) 2011-01-19
US9587011B2 (en) 2017-03-07
DK2274335T3 (en) 2015-08-17

Similar Documents

Publication Publication Date Title
US9598482B2 (en) Monoclonal antibodies capable of reacting with a plurality of influenza virus A subtypes
US9243054B2 (en) Monoclonal antibodies having homosubtype cross-neutralization properties against influenza A viruses subtype H1
EP2793945B1 (en) Antibodies useful in passive influenza immunization
KR20140112495A (ko) 인플루엔자 a 바이러스 특이적 항체
EP2438088A1 (en) Monoclonal antibodies as a medicament for the therapeutic and/or prophylactic treatment of swine -origin influenza a (h1n1) virus (s-oiv) infections
US20190345230A1 (en) Broad-spectrum monoclonal anti-flu b antibody and uses thereof

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980117842.2

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09722394

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: MX/A/2010/010120

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 12922850

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 12010502117

Country of ref document: PH

WWE Wipo information: entry into national phase

Ref document number: 2011500336

Country of ref document: JP

Ref document number: 2718923

Country of ref document: CA

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: PI 2010004341

Country of ref document: MY

WWE Wipo information: entry into national phase

Ref document number: 588238

Country of ref document: NZ

WWE Wipo information: entry into national phase

Ref document number: 2009227567

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 6472/CHENP/2010

Country of ref document: IN

Ref document number: DZP2010000624

Country of ref document: DZ

ENP Entry into the national phase

Ref document number: 20107023021

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 201071087

Country of ref document: EA

WWE Wipo information: entry into national phase

Ref document number: 2009722394

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2009227567

Country of ref document: AU

Date of ref document: 20090316

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: PI0909123

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20100917